Oligosaccharide synthesis by affinity separation based on molecular recognition between podand ether and ammonium ion

被引:31
作者
Fukase, K [1 ]
Takashina, M [1 ]
Hori, Y [1 ]
Tanaka, D [1 ]
Tanaka, K [1 ]
Kusumoto, S [1 ]
机构
[1] Osaka Univ, Grad Sch Sci, Dept Chem, Toyonaka, Osaka 5600043, Japan
关键词
oligosaccharide synthesis; affinity separation; high throughput synthesis; linker; glycosylation;
D O I
10.1055/s-2005-872269
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We previously reported a new synthetic methodology termed 'synthesis based on affinity separation' (SAS) in which the desired tagged compound was separated from the reaction mixture by solid-phase extraction using specific molecular recognition of the tag. The interaction between a crown ether tag and polymer-supported ammonium ion was initially employed for SAS. In the present study, a new SAS method using a podand-type tag, a pseudo-benzo-31-crown-10 structure, was elaborated for oligosaccharide synthesis. The podand tag was much easier to synthesize than the corresponding crown ether. The podand moiety was attached to the monosaccharide residue via appropriate linkers. After glycosylation of the tagged monosaccharide with a glycosyl donor, the reaction mixture was subjected to the affinity separation. The desired compounds possessing the podand tag were effectively separated by the affinity between the podand and the ammonium ion. Continuous flow synthesis by integration of a microreactor and the present SAS system was applied for high throughput oligosaccharide synthesis.
引用
收藏
页码:2342 / 2346
页数:5
相关论文
共 20 条
[1]   Fluorous methods for synthesis and separation of organic molecules [J].
Curran, DP .
PURE AND APPLIED CHEMISTRY, 2000, 72 (09) :1649-1653
[2]  
Egusa K, 1997, SYNLETT, P675
[3]   In situ generation of Fmoc-amino acid chlorides using bis(trichloromethyl) carbonate and its utilization for difficult couplings in solid-phase peptide synthesis [J].
Falb, E ;
Yechezkel, T ;
Salitra, Y ;
Gilon, C .
JOURNAL OF PEPTIDE RESEARCH, 1999, 53 (05) :507-517
[4]  
FUKASE K, 1990, TETRAHEDRON LETT, V31, P389
[5]   4-PIVALOYLAMINOBENZYL ETHER, A NEW TEMPORARY PROTECTION FOR HYDROXYL FUNCTIONS [J].
FUKASE, K ;
YOSHIMURA, T ;
HASHIDA, M ;
KUSUMOTO, S .
TETRAHEDRON LETTERS, 1991, 32 (32) :4019-4022
[6]   p-Nitrophenyl group for anomeric protection of oligosaccharides, selective oxidative cleavage via p-acetamidophenyl glycosides [J].
Fukase, K ;
Yasukochi, T ;
Nakai, Y ;
Kusumoto, S .
TETRAHEDRON LETTERS, 1996, 37 (19) :3343-3344
[7]  
Fukase K, 1999, SYNLETT, P1074
[8]  
FUKASE K, ACS S SERIES, V892
[9]  
Fukase Y, 2001, SYNLETT, P1693
[10]   Chemistry in microstructured reactors [J].
Jähnisch, K ;
Hessel, V ;
Löwe, H ;
Baerns, M .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (04) :406-446